哌唑嗪与可乐定的相互作用。

P A van Zwieten, E Lam, P B Timmermans
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引用次数: 7

摘要

1. 研究了哌唑嗪与可乐定在麻醉大鼠、麻醉大鼠和麻醉猫体内的相互作用。2. 哌唑嗪可能通过中枢肾上腺素受体水平的拮抗作用,降低了麻醉大鼠的可乐定诱导的降压作用。3.在有髓鞘的大鼠中,刺激神经加速剂引起心动过速,可乐定大大减轻了心动过速。普拉唑嗪部分逆转了可乐定的拮抗作用,表明普拉唑嗪除了对突触后α受体起主要作用外,还具有一定程度的突触前活性。哌嗪的活性高于哌唑嗪。4. 猫左椎动脉注射可乐定后,经同样途径给药的普拉唑嗪显著降低了可乐定的中枢性降压作用。静脉注射哌唑嗪并没有降低可乐定的中枢性降压作用。因此,这种对抗是由一种中枢机制引起的。5. 同时使用可乐定和普拉嗪治疗高血压不仅是不合理的,而且考虑到药物之间的相互作用,这可能会导致可乐定的降压效力降低,因此应该予以劝阻。
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The interaction between prazosin and clonidine.

1. The interaction between prazosin and clonidine was studied in anaesthetized rats, pithed rats and in anaesthetized cats. 2. Prazosin diminished the clonidine-induced hypotensive effect in anaesthetized rats, probably via an antagonism at the level of central alpha-adrenoreceptors. 3. In pithed rats, stimulation of the Nervi accelerantes caused tachycardia, which was diminished considerably by clonidine. The antagonism by clonidine was partly reversed by prazosin, suggesting that prazosin possesses a certain degree of presynaptic activity apart from its predominant effect at the postsynaptic alpha-receptor. Piperoxan was more active than prazosin. 4. The central hypotensive effect of clonidine, injected into the left vertebral artery of cats was significantly reduced by prazosin, administered before clonidine via the same route. Intravenously injected prazosin did not diminish the central hypotensive effect of clonidine. The antagonism is, therefore, caused by a central mechanism. 5. The combined application of clonidine and prazosin in antihypertensive treatment is probably not only irrational but ought to be discouraged in view of the interaction between the drugs, which leads to a reduced antihypertensive potency of clonidine.

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Proceedings of the Fifth Meeting of the International Society of Hypertension, Paris, 12-14 June 1978. Brain catecholamines and catecholamine-synthesizing enzymes in renovascular hypertension in the rat. Enhanced hypothalamic noradrenaline biosynthesis in Goldblatt I renovascular hypertension. Definitive evidence for renin in rat brain by affinity chromatographic separation from protease. Renal release of active and inactive renin in essential and renovascular hypertension.
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